About this trial
This study hypothesizes that approximately 50% of rectal cancer patients can preserve their rectum using a watch-and-wait strategy if they achieve a complete or near-complete clinical response to total neoadjuvant therapy (TNT). The objective is to determine whether the complications, quality of life, and survival rates of rectal cancer patients who have achieved a complete or near-complete clinical response to TNT, followed by a watch-and-wait approach, are comparable to those of patients who undergo surgery first. Additionally, the study aims to identify potential prognostic and predictive markers for rectal cancer and examine survival rates and factors influencing responses to chemoradiotherapy (CRT) or TNT.
The study is divided into two parts:
\*\*Part One:\*\* Participants with cT1N1, T2-T3 N0-1 rectal cancer, MRF-, and EMVI-, with surgery as one of the possible first-line treatment options, will be randomized into two groups. The experimental group will consist of participants receiving TNT, including CRT and consolidation chemotherapy (Ch). If these participants achieve a complete or near-complete clinical response, they will be observed using a watch-and-wait strategy, which is a non-operative approach. The control group will consist of participants who undergo surgical treatment initially.
\*\*Part Two:\*\* All participants with rectal cancer who have received CRT or TNT will be included. Additionally, participants diagnosed with rectal cancer who are scheduled for CRT or TNT but declined to participate in Part One or do not meet the inclusion criteria will also be included.
Eligibility criteria
Qualifiers
Over 18 years of age.
Participants who agreed to participate in the study signed an informed consent form.
The Eastern Cooperative Oncology Group (ECOG) score ranges from 0 to 2.
Pathologically confirmed rectal adenocarcinoma.
Disqualifiers
Prior ST or Ch.
Participants who are not eligible for pelvic MRI.
Participants who have had a malignancy in the last 5 years, except for treatment for basal cell or squamous cell skin cancer or in situ cervical cancer.
ECOG status ≥ 3.
Trial design
Treatments tested in this trial
- Radiation Therapy
- Chemoradiotherapy
- Consolidation Chemotherapy
- Surgery
- Part two
- Adjuvant treatment
Treatment groups
Sponsors and collaborators
National Cancer Center Affiliate of Vilnius University Hospital Santaros Klinikos
Lead sponsor
Vilnius University
Collaborator
Tomas Poskus, Faculty of Medicine, Vilnius University
Collaborator
Vilnius University Hospital Santaros Klinikos
Collaborator
Research Council of Lithuania
Collaborator